Canonical Allele Identifier: CA114580
Gene: UBIAD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 861
ClinVar RCV Id: RCV000000909
dbSNP Id: rs118203950

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11273866A>G , CM000663.2:g.11273866A>G GRCh38
NC_000001.10:g.11333923A>G , CM000663.1:g.11333923A>G GRCh37
NC_000001.9:g.11256510A>G NCBI36
NG_009443.1:g.5669A>G
NG_009443.2:g.5669A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376810.6:c.335A>G MANE Select ENSP00000366006.5:p.Asp112Gly
ENST00000376804.2:c.335A>G ENSP00000366000.1:p.Asp112Gly
ENST00000376810.5:c.335A>G ENSP00000366006.5:p.Asp112Gly
NM_013319.2:c.335A>G NP_037451.1:p.Asp112Gly
XM_006710590.2:c.335A>G XP_006710653.1:p.Asp112Gly
XM_011541304.1:c.335A>G XP_011539606.1:p.Asp112Gly
XR_946616.1:n.669A>G
NM_001330349.1:c.335A>G NP_001317278.1:p.Asp112Gly
NM_001330350.1:c.335A>G NP_001317279.1:p.Asp112Gly
XR_946616.3:n.669A>G
NM_001330349.2:c.335A>G NP_001317278.1:p.Asp112Gly
NM_001330350.2:c.335A>G NP_001317279.1:p.Asp112Gly
NM_013319.3:c.335A>G MANE Select NP_037451.1:p.Asp112Gly